A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448326



Internal ID21105879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19533691..19534003hg38UCSC Ensembl
chr11:19555238..19555550hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988720
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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